Canonical Allele Identifier: CA2755144096

Gene: CAV3 SSUH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8734384_8734469del , CM000665.2:g.8734384_8734469del	GRCh38
NC_000003.11:g.8776070_8776155del , CM000665.1:g.8776070_8776155del	GRCh37
NC_000003.10:g.8751070_8751155del	NCBI36
NG_008797.2:g.5575_5660del , LRG_329:g.5575_5660del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343849.3:c.114+394_114+479del (CAV3) MANE Select	ENSP00000341940.2:n.114+394_114+479del
ENST00000343849.2:c.114+394_114+479del (CAV3)	ENSP00000341940.2:n.114+394_114+479del
ENST00000397368.2:c.114+394_114+479del (CAV3)	ENSP00000380525.2:n.114+394_114+479del
ENST00000435138.5:c.64+7992_64+8077del (SSUH2)	ENSP00000412333.1:n.64+7992_64+8077del
ENST00000472766.1:n.155+394_155+479del (CAV3)
ENST00000478513.1:n.335+7992_335+8077del (SSUH2)
NM_001234.4:c.114+394_114+479del (CAV3)	NP_001225.1:n.114+394_114+479del
NM_033337.2:c.114+394_114+479del , LRG_329t1:c.114+394_114+479del (CAV3)	NP_203123.1:n.114+394_114+479del
XR_940435.1:n.330+7992_330+8077del (SSUH2)
XM_017006530.1:c.-283+7992_-283+8077del (SSUH2)	XP_016862019.1:n.-283+7992_-283+8077del
NM_001234.5:c.114+394_114+479del (CAV3)	NP_001225.1:n.114+394_114+479del
NM_033337.3:c.114+394_114+479del (CAV3) MANE Select	NP_203123.1:n.114+394_114+479del